NL7907497A - 2-broombenzylesters en hun toepassing als pesticiden. - Google Patents
2-broombenzylesters en hun toepassing als pesticiden. Download PDFInfo
- Publication number
- NL7907497A NL7907497A NL7907497A NL7907497A NL7907497A NL 7907497 A NL7907497 A NL 7907497A NL 7907497 A NL7907497 A NL 7907497A NL 7907497 A NL7907497 A NL 7907497A NL 7907497 A NL7907497 A NL 7907497A
- Authority
- NL
- Netherlands
- Prior art keywords
- esters
- hydrogen
- bromobenzyl
- group
- chlorine
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title description 9
- -1 2-bromobenzyl ester Chemical class 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 29
- 239000000460 chlorine Chemical group 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 11
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Chemical group 0.000 claims description 8
- 239000011737 fluorine Substances 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 125000006280 2-bromobenzyl group Chemical group [H]C1=C([H])C(Br)=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
- 241000238631 Hexapoda Species 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 230000000361 pesticidal effect Effects 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
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- 239000011149 active material Substances 0.000 description 8
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- 241000255925 Diptera Species 0.000 description 7
- 241000238876 Acari Species 0.000 description 5
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- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 150000002431 hydrogen Chemical group 0.000 description 5
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- 239000000654 additive Substances 0.000 description 4
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- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 241001425390 Aphis fabae Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 241000255967 Helicoverpa zea Species 0.000 description 3
- 241000256250 Spodoptera littoralis Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
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- 239000002202 Polyethylene glycol Substances 0.000 description 1
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- 239000003513 alkali Substances 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
- C07C17/14—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms in the side-chain of aromatic compounds
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- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7840420 | 1978-10-13 | ||
| GB7840420 | 1978-10-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL7907497A true NL7907497A (nl) | 1980-04-15 |
Family
ID=10500306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL7907497A NL7907497A (nl) | 1978-10-13 | 1979-10-10 | 2-broombenzylesters en hun toepassing als pesticiden. |
Country Status (8)
| Country | Link |
|---|---|
| BE (1) | BE879142A (fr) |
| CH (1) | CH643230A5 (fr) |
| DE (1) | DE2941332A1 (fr) |
| FR (1) | FR2438645A1 (fr) |
| GB (1) | GB2035301B (fr) |
| IT (1) | IT1124604B (fr) |
| LU (1) | LU81778A1 (fr) |
| NL (1) | NL7907497A (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3145448A1 (de) * | 1980-11-18 | 1982-08-26 | Kuraray Co., Ltd., Kurashiki, Okayama | Substitutierter bezylester einer 2,2-dimethyl-3-(2,2-dihalogenvinyl)cyclopropancarbonsaeure, diese enthaltende pestizide mittel sowie verfahren zur bekaempfung von schaedlingen |
| EP0228942B1 (fr) * | 1985-12-10 | 1990-05-23 | Roussel-Uclaf | Nouveaux dérivés de l'acide cyclopropane carboxylique à substituant iodé, leur préparation, leur application à la lutte contre les parasites des végétaux et des animaux et les compositions les renfermant |
| FR2601360B2 (fr) * | 1986-07-09 | 1988-11-10 | Roussel Uclaf | Nouveaux derives de l'acide cyclopropane carboxylique a substituant iode, leur preparation, leur application a la lutte contre les parasites des vegetaux et des animaux. |
| FR2591223B1 (fr) * | 1985-12-10 | 1988-03-18 | Roussel Uclaf | Nouveaux derives de l'acide cyclopropane carboxylique a substituant iode, leur preparation, leur application a la lutte contre les parasites des vegetaux et des animaux |
| FR2641275B1 (fr) * | 1988-12-29 | 1991-10-11 | Roussel Uclaf | Nouveaux derives fluores de l'acide 3-ethenyl 2,2-dimethyl cyclopropane carboxylique, leur procede de preparation et leur application comme pesticides |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE786808A (fr) * | 1971-07-28 | 1973-01-29 | Johnson & Son Inc S C | Chrysanthemumates de benzyle |
| GB1533854A (en) * | 1975-03-11 | 1978-11-29 | Shell Int Research | Benzyl thioamides and their use as pesticides |
| DE2658074C2 (de) * | 1976-12-22 | 1986-12-04 | Bayer Ag, 5090 Leverkusen | Cyclopropancarbonsäureester von halogenierten Benzylalkoholen, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Insekten und Akariden |
| US4183950A (en) * | 1976-12-22 | 1980-01-15 | Bayer Aktiengesellschaft | Combating arthropods with 2,2-dimethyl-3-vinyl-cyclopropane carboxylic acid esters of halogenated benzyl alcohols |
-
1979
- 1979-09-17 GB GB7932152A patent/GB2035301B/en not_active Expired
- 1979-10-02 BE BE1/9548A patent/BE879142A/nl not_active IP Right Cessation
- 1979-10-10 NL NL7907497A patent/NL7907497A/nl not_active Application Discontinuation
- 1979-10-11 CH CH915679A patent/CH643230A5/de not_active IP Right Cessation
- 1979-10-11 LU LU81778A patent/LU81778A1/fr unknown
- 1979-10-11 FR FR7925325A patent/FR2438645A1/fr active Granted
- 1979-10-11 DE DE19792941332 patent/DE2941332A1/de active Granted
- 1979-10-11 IT IT26436/79A patent/IT1124604B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| BE879142A (nl) | 1980-04-02 |
| GB2035301A (en) | 1980-06-18 |
| DE2941332C2 (fr) | 1988-10-06 |
| IT1124604B (it) | 1986-05-07 |
| FR2438645B1 (fr) | 1981-08-14 |
| DE2941332A1 (de) | 1980-04-30 |
| CH643230A5 (de) | 1984-05-30 |
| LU81778A1 (fr) | 1980-05-07 |
| FR2438645A1 (fr) | 1980-05-09 |
| IT7926436A0 (it) | 1979-10-11 |
| GB2035301B (en) | 1982-12-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BA | A request for search or an international-type search has been filed | ||
| BB | A search report has been drawn up | ||
| BC | A request for examination has been filed | ||
| BV | The patent application has lapsed |